Product NDC: | 61787-482 |
Proprietary Name: | Nasal Ease Allergy Reliever |
Non Proprietary Name: | Potassium Dichromate |
Active Ingredient(s): | 200 [AU]/5.1g & nbsp; Potassium Dichromate |
Administration Route(s): | NASAL |
Dosage Form(s): | POWDER |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 61787-482 |
Labeler Name: | Health Care Products |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED HOMEOPATHIC |
Start Marketing Date: | 20090803 |
Package NDC: | 61787-482-50 |
Package Description: | 1 BOTTLE in 1 BOX (61787-482-50) > 5.1 g in 1 BOTTLE |
NDC Code | 61787-482-50 |
Proprietary Name | Nasal Ease Allergy Reliever |
Package Description | 1 BOTTLE in 1 BOX (61787-482-50) > 5.1 g in 1 BOTTLE |
Product NDC | 61787-482 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Potassium Dichromate |
Dosage Form Name | POWDER |
Route Name | NASAL |
Start Marketing Date | 20090803 |
Marketing Category Name | UNAPPROVED HOMEOPATHIC |
Labeler Name | Health Care Products |
Substance Name | POTASSIUM DICHROMATE |
Strength Number | 200 |
Strength Unit | [AU]/5.1g |
Pharmaceutical Classes |